J. Miller

发表

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

O. King, K. Wagner, C. Emerson, 2015, Clinical Epigenetics.

Up-regulation of MHC class I expression accompanies but is not required for spontaneous myopathy in dysferlin-deficient SJL/J mice.

J. Dominov, J. Miller, C. Kostek, 2002, The American journal of pathology.

Quantitative switch in integrin expression accompanies differentiation of F9 cells treated with retinoic acid

M. Lotz, C. Burdsal, D. McClay, 1994, Developmental dynamics : an official publication of the American Association of Anatomists.

An upper limit for the branching ratio of the decay Ks → e+e−

M. Chertok, A. Ealet, C. Yèche, 1997 .

The CPLEAR-experiment at CERN

M. Chertok, A. Ealet, C. Yèche, 1997 .

CPLEAR results on the CP parameters of neutral kaons decaying to π+π−π0

M. Chertok, A. Ealet, C. Yèche, 1997 .

Experimental measurement of the ratio in antiproton annihilations at rest in gaseous hydrogen at 15 and 27 bar

M. Chertok, A. Ealet, C. Yèche, 1997 .

Diseased muscles that lack dystrophin or laminin-α2 have altered compositions and proliferation of mononuclear cell populations

M. Girgenrath, J. Miller, C. Kostek, 2005, BMC neurology.

Pro‐ and Anti‐apoptotic Members of the Bcl‐2 Family in Skeletal Muscle: A Distinct Role for Bcl‐2 in Later Stages of Myogenesis

J. Dominov, J. Miller, C. A. Houlihan-Kawamoto, 2001 .

Does the road to muscle rejuvenation go through Notch?

C. Emerson, J. Miller, 2003, Science of aging knowledge environment : SAGE KE.

Muscle-specific BCL2 expression ameliorates muscle disease in laminin {alpha}2-deficient, but not in dystrophin-deficient, mice.

J. Dominov, M. Beermann, J. Miller, 2005, Human molecular genetics.

Proximity ligation assay to detect DUX4 protein in FSHD1 muscle: a pilot study

M. Beermann, S. Homma, J. Miller, 2022, BMC research notes.

First observation of a particle - anti-particle asymmetry in the decay of neutral kaons into pi0 pi0

M. Chertok, A. Ealet, T. Schietinger, 1996 .

Muscle-speciﬁc BCL2 expression ameliorates muscle disease in laminin a 2-deﬁcient, but not in dystrophin-deﬁcient, mice

J. Dominov, M. Beermann, J. Miller, 2005 .

Regeneration of transgenic skeletal muscles with altered timing of expression of the basic helix-loop-helix muscle regulatory factor MRF4.

J. Dominov, G. Pavlath, J. Miller, 2003, The American journal of pathology.

Acetylcholine receptors from Torpedo californica membrane vesicles are metabolized after fusion with cultured mammalian muscle cells

Z. Hall, J. Miller, 1984, Brain Research.

Downstream events initiated by expression of FSHD-associated DUX4: Studies of nucleocytoplasmic transport, γH2AX accumulation, and Bax/Bak-dependence

F. Boyce, Bess M Miller, S. Homma, 2022, Biology open.

Regulation of the Genes Involved in the Utilization of Molybdenum

J. Miller, N. K. Amy, 1988 .

Cell diversification within the myogenic lineage: In vitro generation of two types of myoblasts from a single myogenic progenitor cell

F. Stockdale, D. Schafer, J. Miller, 1987, Cell.

Ku70 regulates Bax-mediated pathogenesis in laminin-alpha2-deficient human muscle cells and mouse models of congenital muscular dystrophy.

J. Miller, V. Vishnudas, 2009, Human molecular genetics.

Myogenic Enhancers Regulate Expression of the Facioscapulohumeral Muscular Dystrophy-Associated DUX4 Gene

M. Beermann, Peter L Jones, T. Jones, 2014, Molecular and Cellular Biology.

TWEAK, via its receptor Fn14, is a novel regulator of mesenchymal progenitor cells and skeletal muscle regeneration

M. Girgenrath, M. Scott, R. Flavell, 2006, The EMBO journal.

Isolation and Characterization of an Avian Slow Myosin Heavy Chain Gene Expressed during Embryonic Skeletal Muscle Fiber Formation*

F. Stockdale, R. Wade, J. Feldman, 1996, The Journal of Biological Chemistry.

Prdm1 (Blimp-1) and the Expression of Fast and Slow Myosin Heavy Chain Isoforms during Avian Myogenesis In Vitro

M. Girgenrath, M. Beermann, J. Miller, 2010, PloS one.

Myoblasts, myosins, MyoDs, and the diversification of muscle fibers

J. Miller, 1991, Neuromuscular Disorders.

Myoblast diversity in skeletal myogenesis: How much and to what end?

J. Miller, 1992, Cell.

Slow and Fast Myosin Heavy Three Types of Myotubes in Chain Content Defines Early Muscle Cell Cultures

M. Crow, F. Stockdale, J. Miller, 1985 .

Coding sequence, chromosomal localization, and expression pattern of Nrf1: the mouse homolog of Drosophila erect wing

L. Schaefer, J. Miller, H. Engman, 2000, Mammalian Genome.

Immortalization of mouse myogenic cells can occur without loss of p16INK4a, p19ARF, or p53 and is accelerated by inactivation of Bax

M. Girgenrath, J. Dominov, J. Nowak, 2004, BMC Cell Biology.

Immortalized myogenic cells from congenital muscular dystrophy type1A patients recapitulate aberrant caspase activation in pathogenesis: a new tool for MDC1A research

Soonsang Yoon, W. Wright, P. Schneiderat, 2013, Skeletal Muscle.

Bcl-2 Expression Identifies an Early Stage of Myogenesis and Promotes Clonal Expansion of Muscle Cells

J. Dominov, J. Miller, J. J. Dunn, 1998, The Journal of cell biology.

The role of apoptosis in neuromuscular diseases and prospects for anti-apoptosis therapy.

M. Girgenrath, J. Miller, 2006, Trends in molecular medicine.

Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4

F. Boyce, M. Beermann, S. Homma, 2016, Skeletal Muscle.

Expression of FSHD-related DUX4-FL alters proteostasis and induces TDP-43 aggregation

F. Boyce, M. Beermann, S. Homma, 2015, Annals of clinical and translational neurology.

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis.

O. King, L. Kunkel, K. Wagner, 2012, Human molecular genetics.

A unique library of myogenic cells from facioscapulohumeral muscular dystrophy subjects and unaffected relatives: family, disease and cell function

Sachiko Homma, L. Kunkel, K. Wagner, 2011, European Journal of Human Genetics.

Functional domains of the FSHD-associated DUX4 protein

M. Beermann, S. Ishimaru, H. Mitsuhashi, 2018, Biology Open.

Pathology is alleviated by doxycycline in a laminin‐α2–null model of congenital muscular dystrophy

M. Girgenrath, M. Beermann, S. Homma, 2008, Annals of neurology.

Acceleration of somitic myogenesis in embryos of myogenin promoter‐MRF4 transgenic mice

J. Dominov, Zhimin Zhu, J. Miller, 1996, Developmental dynamics : an official publication of the American Association of Anatomists.

Erratum: Subthreshold pion production with associated multiplicity selection in the reaction La139+La139+X (Physical Review Letters (1987) 59, 4, (519))

L. Schroeder, W. Benenson, G. Roche, 1987 .

Cellular and molecular diversity in skeletal muscle development: News from in vitro and in vivo

J. Miller, E. A. Everitt, T. H. Smith, 1993, BioEssays : news and reviews in molecular, cellular and developmental biology.

Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy

O. King, K. Wagner, C. Emerson, 2015, Clinical Epigenetics.

Disruption of the COP9 Signalosome Csn2 Subunit in Mice Causes Deficient Cell Proliferation, Accumulation of p53 and Cyclin E, and Early Embryonic Death

X. Deng, Karin Lykke-Andersen, N. Wei, 2003, Molecular and Cellular Biology.

Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4

F. Boyce, M. Beermann, S. Homma, 2016, Skeletal Muscle.

Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers

F. Boyce, M. Beermann, S. Ishimaru, 2019, Scientific Reports.

What muscle cells know that nerves don't tell them

F. Stockdale, J. Miller, 1987, Trends in Neurosciences.

Inhibition of apoptosis improves outcome in a model of congenital muscular dystrophy.

M. Girgenrath, J. Dominov, J. Miller, 2004, The Journal of clinical investigation.

Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy.

M. Beermann, S. Homma, J. Miller, 2011, Human molecular genetics.

Measurement of the CP-violation parameter η00 using tagged K0 and K0

M. Chertok, A. Ealet, T. Schietinger, 1998 .

Measurements of dilepton production in nucleon-nucleon interactions

Z. F. Wang, A. Letessier-Selvon, R. Welsh, 1994 .

Myogenesis and the intermediate filament protein, nestin.

J. Miller, J. Dominov, J. Miller, 1994, Developmental biology.

Aberrant Caspase Activation in Laminin-α2-Deficient Human Myogenic Cells is Mediated by p53 and Sirtuin Activity

Soonsang Yoon, M. Beermann, M. Bachschmid, 2017, Journal of neuromuscular diseases.

Intermediate filaments in cardiac myogenesis: nestin in the developing mouse heart.

J. Miller, J. Dominov, J. Miller, 1995, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Myogenic programs of mouse muscle cell lines: expression of myosin heavy chain isoforms, MyoD1, and myogenin

J. Miller, J. Miller, J B Miller, 1990, The Journal of cell biology.

Seeking muscle stem cells.

J. Miller, J. Dominov, Laura Schaefer, 1999, Current topics in developmental biology.

Somite subdomains, muscle cell origins, and the four muscle regulatory factor proteins

J. Miller, T. H. Smith, J. Miller, 1994, The Journal of cell biology.

A unique pattern of expression of the four muscle regulatory factor proteins distinguishes somitic from embryonic, fetal and newborn mouse myogenic cells.

S. Rhodes, J. Miller, T. H. Smith, 1993, Development.

Isolation and Characterization of an Avian Slow Myosin Heavy Chain Gene Expressed during Embryonic Skeletal Muscle Fiber Formation*

F. Stockdale, R. Wade, J. Feldman, 1996, The Journal of Biological Chemistry.

Membrane fluidity and chemotaxis: effects of temperature and membrane lipid composition on the swimming behavior of Salmonella typhimurium and Escherichia coli.

D. Koshland, J. Miller, J. B. Miller, 1977, Journal of molecular biology.

Effects of cyanine dye membrane probes on cellular properties

D. Koshland, J. Miller, 1978, Nature.

Ku70 regulates Bax-mediated pathogenesis in laminin-alpha2-deficient human muscle cells and mouse models of congenital muscular dystrophy.

J. Miller, V. Vishnudas, 2009, Human molecular genetics.

Efficient system for upstream mRNA trans-splicing to generate covalent, head-to-tail, protein multimers

F. Boyce, M. Beermann, S. Ishimaru, 2019, Scientific Reports.

Bcl-2 Expression Identifies an Early Stage of Myogenesis and Promotes Clonal Expansion of Muscle Cells

J. Dominov, J. Miller, J. J. Dunn, 1998, The Journal of cell biology.